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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1054326생성일: 2026년 10월 27일

3-Chlorobenzaldehyde → [6-Chloro-2-(3-chloro-phenyl)-imidazo[1,2-a]pyridin-3-yl]-cyclopropyl-amine

https://huagongshe.com/reaction/1054326

반응식

참여 물질

역할이름HCID투입량
반응물3-ChlorobenzaldehydeHCID 11477—
반응물2-Amino-5-chloropyridineHCID 66174—
반응물p-Toluenesulfonic acid monohydrateHCID 521998—
반응물IsocyanocyclopropaneHCID 2758008—
용매MethanolHCID 887—
생성물[6-Chloro-2-(3-chloro-phenyl)-imidazo[1,2-a]pyridin-3-yl]-cyclopropyl-amineHCID 7476378318.2%

반응 단계

5-chloropyridin-2-amine (100 mg, 778 μmol, Eq: 1.00), 3-chlorobenzaldehyde (115 mg, 93.0 μl, 817 μmol, Eq: 1.05) and p-toluenesulfonic acid monohydrate (44.4 mg, 233 μmol, Eq: 0.3) were dissolved in MeOH (1.00 mL) and the intensive yellow solution was stirred for 10 min. To this yellow solution was added dropwise isocyanocyclopropane (52.2 mg, 47.4 μL, 778 μmol, Eq: 1.00) and the corresponding yellow solution was stirred for 2 h. The solvent was removed and the dark red oil was purified twice by flash column chromatography (ethyl acetate in hexanes) to give the product as yellow solid (45 mg, 18.2%). LC/MS (acid polar): 318.1 [M+H]+; 1H-NMR (CDCl3): δ 8.50 (s, 1H), 8.21 (s, 1H), 8.14 (d, 1H), 7.58 (d, 1H), 7.49 (t, 1H), 7.38 (d, 1H), 7.28 (d, 1H), 5.44 (s, 1H), 2.70 (m, 1H), 0.46-0.39 (m, 4H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09394304B2
출처 데이터셋uspto-grants-2016_07
ORD IDord-d91c3aad364748d1bede9c65528fd0ba
출처 메모uspto-grants-2016_07